A diabetogenic alloxan regimen produced lesions in all stomachs of treated
animals, either rats (200 mg.kg(-1) s.c.) or mice (400 mg.kg(-1) i.p.). In
control animals, the lesions, when developed (i.e. 24 h following applicati
on), appear to be quite sustained, and consistently present also after 1 or
2 weeks. The application of the pentadecapeptide BPC 157 (10 mu g or 10 ng
.kg(-1) i.p. coadministered together with alloxan) would significantly atte
nuate these lesions' appearance. This beneficial effect seems to be present
in either rats or mice and in either of the tested intervals. Importantly,
the beneficial effect seems to be shared by both microgram and nanogram re
gimens. (C) 1999 Elsevier Science Ltd. Published by Editions scientifiques
et medicales Elsevier SAS.